GLA anticorps (AA 218-275)

N° du produit ABIN5647751

Cet anticorps anti-GLA est un anticorps Lapin Polyclonal détectant GLA dans WB. Adapté pour Souris.

Aperçu rapide pour GLA anticorps (AA 218-275) (ABIN5647751)

Antigène: GLA (Galactosidase, alpha (GLA))

Reactivité: Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp GLA est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-GLA anticorps

Épitope: AA 218-275

Purification: Antigen affinity purified

Immunogène: Amino acids 218-275 (DIQYYCNHWRNFDDVYDSWESIKNILSWTVVYQKEIVEVA-mouse) were used as the immunogen for the Gla antibody.

Isotype: IgG

Information d'application

Indications d'application: Optimal dilution of the Gla antibody should be determined by the researcher.\. Western blot: 0.5-1 μg/mL

Restrictions: For Research Use only

Stockage

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Stock: -20 °C

Stockage commentaire: After reconstitution, the Gla antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.

Détails sur GLA

Antigène: GLA (Galactosidase, alpha (GLA))

Autre désignation: Gla / Galactosidase alpha

Sujet: Alpha-galactosidase is a glycoside hydrolase enzyme that encoded by the GLA gene. This gene is a homodimeric glycoprotein that hydrolyses the terminal alpha-galactosyl moieties from glycolipids and glycoproteins. This enzyme predominantly hydrolyzes ceramide trihexoside, and it can catalyze the hydrolysis of melibiose into galactose and glucose. A variety of mutations in this gene affect the synthesis, processing, and stability of this enzyme, which causes Fabry disease, a rare lysosomal storage disorder that results from a failure to catabolize alpha-D-galactosyl glycolipid moieties.

UniProt: P51569

Pathways: SARS-CoV-2 Protein Interactome